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Sotalol Pediatric Decision Tree and Exposure-Response Relationship Peter Hinderling, OCPB Saul et al. JCP 2001;40:35-43 Saul et al. CPT 2001;69:145-57.

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Presentation on theme: "Sotalol Pediatric Decision Tree and Exposure-Response Relationship Peter Hinderling, OCPB Saul et al. JCP 2001;40:35-43 Saul et al. CPT 2001;69:145-57."— Presentation transcript:

1 Sotalol Pediatric Decision Tree and Exposure-Response Relationship Peter Hinderling, OCPB Saul et al. JCP 2001;40:35-43 Saul et al. CPT 2001;69:145-57 Shi et el. JPK PD 2001;28:555-75

2 Sotalol Adults 1992 : Life threatening VT, VF (Betapace ®) 2000 : Maintenance of SR in sympt. AFIB/AFL (Betapace AF ™) PK: Linear F: 90% Ae/D=90 % t1/2 = 12 h PK-PD: Linear dl Sotalol : Class III antiarrythmic act. l Sotalol :  -blocking act.

3 Knowledge on Sotalol in Pediatrics in 1999 Published, uncontrolled studies in children using adult doses adjusted for BSA or BW and  =12 h Breakthrough arrhythmias with  =12 h

4 Lipicky Paradigm (Pediatric Summit, Washington, 2002): “ Do what is feasible in children, see what can be extracted and use it.” “ In the case of antiarrhythmics where the demonstration of efficacy even in adults is shaky, it is not reasonable to ask for efficacy in children.”

5 PD Biomarkers Class III / safety: QTc- Interval Class II /safety: Resting RR-Interval

6

7 Written Request PK : Open label, single dose study, 1 dose level, extensive sampling,  6 N,  10 I,  10 PC,  10 SC PK-PD : Open label, multiple ascending dose study, 3 dose levels, sparse sampling,  8 N or  8 I completing

8 Study Protocols

9 Methods Formulation: Syrup, extemporaneous compounding procedure Assay: LC/MS/MS, 0.4 ml blood required ECG: Same type in all sites Baseline values during 8 h dose interval Blinded cardiologist, digitizing pad QTc Fridericia, Bazett Data analysis: Traditional and population approaches PK: Linear 2 CM PK-PD: Linear and Emax models

10 Study Sites and Database Sites 24 sites initiated for PK study 21 sites initiated for PK-PD study 59 patients enrolled (34 in PK study, 25 in PK-PD study) 54 SVT, 3 VT, 2 SVT & VT Database 58 patients with analyzable PK data ( 9 N, 17 I, 9 PC, 23 SC) 22 patients with analyzable PD data ( 6 N, 8 I, 3 PC, 5 SC)

11 Representative Semilogarithmic Plots of Sotalol Plasma Concentrations

12 Relationship between CL/f and Vc/f and BSA (Empirical Bayes Estimates)

13 Plot of Dose and BSA Normalized AUC vs. BSA for 58 Pediatric Patients and 40 Adults

14 Dose-Response Relationship

15 Impact of BSA on PK

16 Consequential Impact of BSA on PD

17 Representative Plots of Observed QTc Intervals vs. (Empirical Bayes) Predicted Sotalol Concentrations in 4 Individuals

18 Representative Plots of Observed RR Intervals vs. (Empirical Bayes) Predicted Sotalol Concentrations in 4 Individuals

19 Summary of Results PK - Linear and dose proportionate - t1/2  10 hours, independent of BSA - CL/f and Vc/f linearly dependent on BSA - BSA most important covariate - Greater exposure of smallest children (BSA < 0.33 m 2 ) PD, PK-PD - Doses tolerated well - Responses increase dose dependently - Pharmacologically important effects: Class III at 70 mg/m 2,  -blocking at 30 and 70 mg/m 2 - Trend for greater effects in smallest children - Effects linearly correlated with concentrations  -blocking effect increases with BSA

20 Additional Dose Adjustment Factor in N and I

21 Conclusions Exposure-response analysis in children using biomarkers: PS and SC: “Small adults”, similar exposure and response as adults, BSA based dose adjustment appropriate N and I: Subpopulation with larger exposure and response Maturation of kidney Additional dose adjustment required


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